Latency and reactivation of a precore mutant hepatitis B virus in a chronically infected patient

J Hepatol. 1990 Nov;11(3):374-80. doi: 10.1016/0168-8278(90)90224-f.

Abstract

In human patients infected with hepatitis B virus (HBV) seroconversion from HBe to anti-HBe often signals virus elimination. Occasionally, a second viremic phase is observed which may be due to superinfection with a variant or reactivation of a latent virus. To differentiate between these two possibilities we investigated the nucleotide sequences of virus populations from sera of a chronically infected patient who had two distinct viremic phases, one e-antigen positive and one anti-HBe antibody positive. By direct sequencing of amplified HBV C- and pre-S gene sequences we found that the viruses in the two populations differed by only two point mutations, one of which prevents expression of precore derived e-antigen. In the nonviremic phase viral DNA and antigen were found in the liver but nucleocapsid protein expression appeared drastically downregulated. These data demonstrate that HBV can enter a latent phase with low expression of core protein and selection for HBV variants which cannot synthesize e-antigen. This suggests that e-antigen expression can be a critical target for virus elimination and that loss of its expression can prolong chronicity and provoke latency of HBV infection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, Viral / analysis
  • Antigens, Viral / immunology
  • Base Sequence
  • Chronic Disease
  • DNA, Viral / analysis
  • DNA, Viral / genetics
  • Down-Regulation / genetics
  • Gene Expression Regulation, Viral / physiology
  • Hepatitis B / genetics*
  • Hepatitis B / immunology
  • Hepatitis B / physiopathology
  • Hepatitis B e Antigens / genetics
  • Hepatitis B e Antigens / metabolism
  • Hepatitis B virus / genetics*
  • Hepatitis B virus / growth & development
  • Hepatitis B virus / immunology
  • Humans
  • Liver / chemistry
  • Liver / metabolism
  • Liver / pathology
  • Molecular Sequence Data
  • Mutation / genetics
  • Reaction Time / physiology*
  • Viral Core Proteins / genetics
  • Viral Core Proteins / metabolism
  • Virus Activation

Substances

  • Antigens, Viral
  • DNA, Viral
  • Hepatitis B e Antigens
  • Viral Core Proteins